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HYPERSTETHOSCOPE, MODEL Z 00

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801165
510(k) Type
Traditional
Applicant
DEMONBINDER ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1980
Days to Decision
8 days

HYPERSTETHOSCOPE, MODEL Z 00

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801165
510(k) Type
Traditional
Applicant
DEMONBINDER ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1980
Days to Decision
8 days